SNAP91 (synaptosome associated protein 91) - Rat Genome Database

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Gene: SNAP91 (synaptosome associated protein 91) Homo sapiens
Analyze
Symbol: SNAP91
Name: synaptosome associated protein 91
RGD ID: 731271
HGNC Page HGNC:14986
Description: Predicted to enable several functions, including clathrin adaptor activity; clathrin heavy chain binding activity; and phosphatidylinositol binding activity. Acts upstream of or within regulation of clathrin-dependent endocytosis. Predicted to be located in several cellular components, including postsynaptic density; presynaptic endosome; and presynaptic membrane. Predicted to be extrinsic component of endosome membrane. Predicted to be active in several cellular components, including Schaffer collateral - CA1 synapse; cytoplasmic vesicle; and parallel fiber to Purkinje cell synapse. Predicted to be extrinsic component of presynaptic endocytic zone membrane. Biomarker of Alzheimer's disease.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: 91 kDa synaptosomal-associated protein; AP180; assembly protein, 180kDa; CALM; clathrin coat assembly protein AP180; clathrin coat-associated protein AP180; DKFZp781O0519; KIAA0656; phosphoprotein F1-20; synaptosomal-associated protein, 91kDa homolog; synaptosome associated protein 91kDa
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38683,552,885 - 83,709,393 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl683,552,880 - 83,709,691 (-)EnsemblGRCh38hg38GRCh38
GRCh37684,262,604 - 84,419,112 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36684,319,332 - 84,475,495 (-)NCBINCBI36Build 36hg18NCBI36
Build 34684,319,331 - 84,475,495NCBI
Celera684,695,893 - 84,852,438 (-)NCBICelera
Cytogenetic Map6q14.2NCBI
HuRef681,492,256 - 81,648,799 (-)NCBIHuRef
CHM1_1684,360,208 - 84,516,740 (-)NCBICHM1_1
T2T-CHM13v2.0684,776,120 - 84,932,636 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. Changed clathrin regulatory proteins in the brains of Alzheimer's disease patients and animal models. Cao Y, etal., J Alzheimers Dis. 2010;22(1):329-42. doi: 10.3233/JAD-2010-100162.
2. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
3. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
4. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
5. Calpain hydrolysis of alpha- and beta2-adaptins decreases clathrin-dependent endocytosis and may promote neurodegeneration. Rudinskiy N, etal., J Biol Chem. 2009 May 1;284(18):12447-58. doi: 10.1074/jbc.M804740200. Epub 2009 Feb 24.
6. Synaptic vesicle endocytosis. Saheki Y and De Camilli P, Cold Spring Harb Perspect Biol. 2012 Sep 1;4(9):a005645. doi: 10.1101/cshperspect.a005645.
Additional References at PubMed
PMID:8063760   PMID:8619474   PMID:9110174   PMID:9734811   PMID:10430869   PMID:10436022   PMID:10579202   PMID:10748223   PMID:11779129   PMID:12477932   PMID:12493563   PMID:12538641  
PMID:12732633   PMID:12750376   PMID:12807910   PMID:12847086   PMID:14574404   PMID:15345747   PMID:15489334   PMID:15555551   PMID:16254249   PMID:16344560   PMID:16413285   PMID:17043677  
PMID:17762867   PMID:19086053   PMID:19450545   PMID:20379614   PMID:20511563   PMID:21808019   PMID:21813615   PMID:21873635   PMID:22479182   PMID:22639918   PMID:22939629   PMID:23092984  
PMID:23678185   PMID:26186194   PMID:26204806   PMID:26412491   PMID:27574975   PMID:28514442   PMID:29997244   PMID:31980649   PMID:32296183   PMID:32812023   PMID:33961781   PMID:34369648  
PMID:34709727   PMID:35063084   PMID:35384245   PMID:36373674  


Genomics

Comparative Map Data
SNAP91
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38683,552,885 - 83,709,393 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl683,552,880 - 83,709,691 (-)EnsemblGRCh38hg38GRCh38
GRCh37684,262,604 - 84,419,112 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36684,319,332 - 84,475,495 (-)NCBINCBI36Build 36hg18NCBI36
Build 34684,319,331 - 84,475,495NCBI
Celera684,695,893 - 84,852,438 (-)NCBICelera
Cytogenetic Map6q14.2NCBI
HuRef681,492,256 - 81,648,799 (-)NCBIHuRef
CHM1_1684,360,208 - 84,516,740 (-)NCBICHM1_1
T2T-CHM13v2.0684,776,120 - 84,932,636 (-)NCBIT2T-CHM13v2.0
Snap91
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39986,647,976 - 86,762,766 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl986,647,976 - 86,762,707 (-)EnsemblGRCm39 Ensembl
GRCm38986,765,923 - 86,880,734 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl986,765,923 - 86,880,654 (-)EnsemblGRCm38mm10GRCm38
MGSCv37986,659,239 - 86,775,207 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36986,562,350 - 86,678,320 (-)NCBIMGSCv36mm8
Celera983,843,031 - 83,967,649 (-)NCBICelera
Cytogenetic Map9E3.1NCBI
cM Map946.58NCBI
Snap91
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8896,618,039 - 96,732,763 (-)NCBIGRCr8
mRatBN7.2887,738,056 - 87,852,690 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl887,738,824 - 87,852,367 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx893,418,568 - 93,525,116 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0891,617,774 - 91,724,331 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0889,459,489 - 89,566,103 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0894,447,558 - 94,564,772 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl894,447,550 - 94,564,525 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0893,958,152 - 94,074,269 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4892,033,425 - 92,147,091 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1892,052,879 - 92,166,546 (-)NCBI
Celera887,338,970 - 87,446,775 (-)NCBICelera
Cytogenetic Map8q31NCBI
Snap91
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495541111,175,525 - 11,300,950 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495541111,175,587 - 11,301,145 (-)NCBIChiLan1.0ChiLan1.0
SNAP91
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v25103,646,352 - 103,805,054 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan16101,542,959 - 101,701,653 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0681,441,792 - 81,600,505 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1684,717,271 - 84,875,561 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl684,720,850 - 84,874,407 (-)Ensemblpanpan1.1panPan2
SNAP91
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11243,919,925 - 44,058,315 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1243,919,925 - 44,058,616 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1243,734,660 - 43,872,902 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01244,689,016 - 44,828,781 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1244,689,023 - 44,828,948 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11244,027,843 - 44,166,268 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01243,961,559 - 44,100,121 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01244,138,511 - 44,276,836 (-)NCBIUU_Cfam_GSD_1.0
Snap91
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494679,125,757 - 79,248,750 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365107,223,757 - 7,343,742 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365107,222,200 - 7,345,138 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
SNAP91
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl182,541,018 - 82,698,633 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1182,540,998 - 82,698,652 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2192,790,018 - 92,949,958 (+)NCBISscrofa10.2Sscrofa10.2susScr3
SNAP91
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1138,221,601 - 8,374,205 (-)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_023666040184,439,639 - 184,590,396 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Snap91
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462479910,915,477 - 11,060,312 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462479910,913,834 - 11,060,185 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in SNAP91
57 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 6q14.1-16.1(chr6:82569098-93753476)x1 copy number loss See cases [RCV000052192] Chr6:82569098..93753476 [GRCh38]
Chr6:83278815..94463194 [GRCh37]
Chr6:83335534..94519915 [NCBI36]
Chr6:6q14.1-16.1		 pathogenic
GRCh38/hg38 6q14.2-14.3(chr6:83656740-84305263)x3 copy number gain See cases [RCV000053346] Chr6:83656740..84305263 [GRCh38]
Chr6:84366459..85014981 [GRCh37]
Chr6:84423178..85071700 [NCBI36]
Chr6:6q14.2-14.3		 uncertain significance
GRCh38/hg38 6q14.2-14.3(chr6:83680568-84270992)x3 copy number gain See cases [RCV000053364] Chr6:83680568..84270992 [GRCh38]
Chr6:84390287..84980710 [GRCh37]
Chr6:84447006..85037429 [NCBI36]
Chr6:6q14.2-14.3		 uncertain significance
NM_001242792.1(SNAP91):c.299G>A (p.Arg100Lys) single nucleotide variant Malignant melanoma [RCV000067483] Chr6:83662397 [GRCh38]
Chr6:84372116 [GRCh37]
Chr6:84428835 [NCBI36]
Chr6:6q14.2		 not provided
NM_001242792.1(SNAP91):c.807+751A>T single nucleotide variant Lung cancer [RCV000097223] Chr6:83622550 [GRCh38]
Chr6:84332269 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.1(SNAP91):c.546+567T>A single nucleotide variant Lung cancer [RCV000097224] Chr6:83658432 [GRCh38]
Chr6:84368151 [GRCh37]
Chr6:6q14.2		 uncertain significance
GRCh38/hg38 6q14.1-14.2(chr6:78912019-84096427)x1 copy number loss See cases [RCV000137752] Chr6:78912019..84096427 [GRCh38]
Chr6:79621736..84806146 [GRCh37]
Chr6:79678455..84862865 [NCBI36]
Chr6:6q14.1-14.2		 uncertain significance
GRCh38/hg38 6q13-24.1(chr6:74382807-142040500)x3 copy number gain See cases [RCV000139729] Chr6:74382807..142040500 [GRCh38]
Chr6:75092523..142361637 [GRCh37]
Chr6:75149243..142403330 [NCBI36]
Chr6:6q13-24.1		 pathogenic
GRCh38/hg38 6q14.2-14.3(chr6:83656740-84324523)x3 copy number gain See cases [RCV000140655] Chr6:83656740..84324523 [GRCh38]
Chr6:84366459..85034241 [GRCh37]
Chr6:84423178..85090960 [NCBI36]
Chr6:6q14.2-14.3		 uncertain significance
GRCh38/hg38 6q14.2-14.3(chr6:83664023-84334552)x3 copy number gain See cases [RCV000142064] Chr6:83664023..84334552 [GRCh38]
Chr6:84373742..85044270 [GRCh37]
Chr6:84430461..85100989 [NCBI36]
Chr6:6q14.2-14.3		 uncertain significance
GRCh38/hg38 6q14.2-14.3(chr6:83656740-84324523)x4 copy number gain See cases [RCV000143170] Chr6:83656740..84324523 [GRCh38]
Chr6:84366459..85034241 [GRCh37]
Chr6:84423178..85090960 [NCBI36]
Chr6:6q14.2-14.3		 uncertain significance
GRCh38/hg38 6q14.1-16.1(chr6:75926199-92710793)x1 copy number loss See cases [RCV000143505] Chr6:75926199..92710793 [GRCh38]
Chr6:76635916..93420511 [GRCh37]
Chr6:76692636..93477232 [NCBI36]
Chr6:6q14.1-16.1		 pathogenic
Single allele deletion Immunodeficiency 23 [RCV000210384] Chr6:83145962..84389166 [GRCh37]
Chr6:6q14.1-14.2		 pathogenic
NM_001242792.2(SNAP91):c.1505A>C (p.Glu502Ala) single nucleotide variant not specified [RCV004309047] Chr6:83593669 [GRCh38]
Chr6:84303388 [GRCh37]
Chr6:6q14.2		 uncertain significance
GRCh37/hg19 6q14.2-14.3(chr6:84373742-85044270)x3 copy number gain See cases [RCV000449263] Chr6:84373742..85044270 [GRCh37]
Chr6:6q14.2-14.3		 likely benign
GRCh37/hg19 6q14.2-14.3(chr6:84354004-85044270)x3 copy number gain See cases [RCV000447412] Chr6:84354004..85044270 [GRCh37]
Chr6:6q14.2-14.3		 uncertain significance
GRCh37/hg19 6q14.2-14.3(chr6:84366014-84922654)x3 copy number gain See cases [RCV000448612] Chr6:84366014..84922654 [GRCh37]
Chr6:6q14.2-14.3		 uncertain significance
GRCh37/hg19 6p25.3-q27(chr6:156975-170919482)x3 copy number gain See cases [RCV000512067] Chr6:156975..170919482 [GRCh37]
Chr6:6p25.3-q27		 pathogenic
GRCh37/hg19 6p25.3-q27(chr6:156975-170919482) copy number gain See cases [RCV000510595] Chr6:156975..170919482 [GRCh37]
Chr6:6p25.3-q27		 pathogenic
GRCh37/hg19 6q14.2-14.3(chr6:84364140-85044270)x3 copy number gain See cases [RCV000511181] Chr6:84364140..85044270 [GRCh37]
Chr6:6q14.2-14.3		 conflicting data from submitters
NM_001242792.2(SNAP91):c.2023G>C (p.Gly675Arg) single nucleotide variant not specified [RCV004307939] Chr6:83582348 [GRCh38]
Chr6:84292067 [GRCh37]
Chr6:6q14.2		 uncertain significance
GRCh37/hg19 6q14.2-14.3(chr6:84374492-85044270)x3 copy number gain See cases [RCV000512299] Chr6:84374492..85044270 [GRCh37]
Chr6:6q14.2-14.3		 uncertain significance
GRCh37/hg19 6q13-14.2(chr6:73674612-84829774)x1 copy number loss not provided [RCV000682681] Chr6:73674612..84829774 [GRCh37]
Chr6:6q13-14.2		 pathogenic
GRCh37/hg19 6q14.1-16.1(chr6:81261418-97796269)x3 copy number gain not provided [RCV000682688] Chr6:81261418..97796269 [GRCh37]
Chr6:6q14.1-16.1		 pathogenic
GRCh37/hg19 6q14.2-14.3(chr6:84373742-85044270)x3 copy number gain not provided [RCV000682689] Chr6:84373742..85044270 [GRCh37]
Chr6:6q14.2-14.3		 uncertain significance
Single allele deletion not provided [RCV000677932] Chr6:83319012..91907669 [GRCh37]
Chr6:6q14.1-15		 pathogenic
GRCh37/hg19 6p25.3-q27(chr6:60107-171054786)x3 copy number gain not provided [RCV000745400] Chr6:60107..171054786 [GRCh37]
Chr6:6p25.3-q27		 pathogenic
GRCh37/hg19 6p25.3-q27(chr6:165632-170919470)x3 copy number gain not provided [RCV000745404] Chr6:165632..170919470 [GRCh37]
Chr6:6p25.3-q27		 pathogenic
GRCh37/hg19 6p25.3-q27(chr6:108666-170980171)x3 copy number gain not provided [RCV000745403] Chr6:108666..170980171 [GRCh37]
Chr6:6p25.3-q27		 pathogenic
GRCh37/hg19 6q14.2-14.3(chr6:84348873-85052572)x3 copy number gain not provided [RCV000745882] Chr6:84348873..85052572 [GRCh37]
Chr6:6q14.2-14.3		 benign
GRCh37/hg19 6q14.2-14.3(chr6:84348995-85043919)x3 copy number gain not provided [RCV000745883] Chr6:84348995..85043919 [GRCh37]
Chr6:6q14.2-14.3		 benign
GRCh37/hg19 6q14.2-14.3(chr6:84356242-85043919)x3 copy number gain not provided [RCV000745884] Chr6:84356242..85043919 [GRCh37]
Chr6:6q14.2-14.3		 benign
NM_001242792.2(SNAP91):c.1446G>A (p.Pro482=) single nucleotide variant not provided [RCV000905515] Chr6:83593728 [GRCh38]
Chr6:84303447 [GRCh37]
Chr6:6q14.2		 benign
NM_001242792.2(SNAP91):c.2508T>C (p.Pro836=) single nucleotide variant not provided [RCV000958971] Chr6:83560882 [GRCh38]
Chr6:84270601 [GRCh37]
Chr6:6q14.2		 benign|likely benign
NM_001242792.2(SNAP91):c.2058T>G (p.Thr686=) single nucleotide variant not provided [RCV000969515] Chr6:83582313 [GRCh38]
Chr6:84292032 [GRCh37]
Chr6:6q14.2		 benign
NM_001242792.2(SNAP91):c.2496G>A (p.Ser832=) single nucleotide variant not provided [RCV000885762] Chr6:83560894 [GRCh38]
Chr6:84270613 [GRCh37]
Chr6:6q14.2		 benign
NM_001242792.2(SNAP91):c.1142-6C>G single nucleotide variant not provided [RCV000893599] Chr6:83601605 [GRCh38]
Chr6:84311324 [GRCh37]
Chr6:6q14.2		 benign
NM_001242792.2(SNAP91):c.18C>G (p.Leu6=) single nucleotide variant not provided [RCV000961742] Chr6:83707910 [GRCh38]
Chr6:84417629 [GRCh37]
Chr6:6q14.2		 benign
GRCh37/hg19 6q14.2-14.3(chr6:84369643-85044077)x3 copy number gain not provided [RCV000849732] Chr6:84369643..85044077 [GRCh37]
Chr6:6q14.2-14.3		 uncertain significance
GRCh37/hg19 6q14.2-14.3(chr6:84354003-85052572)x3 copy number gain not provided [RCV000845624] Chr6:84354003..85052572 [GRCh37]
Chr6:6q14.2-14.3		 uncertain significance
NM_001242792.2(SNAP91):c.460G>C (p.Gly154Arg) single nucleotide variant not specified [RCV004301627] Chr6:83659085 [GRCh38]
Chr6:84368804 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.495A>G (p.Leu165=) single nucleotide variant not provided [RCV000910935] Chr6:83659050 [GRCh38]
Chr6:84368769 [GRCh37]
Chr6:6q14.2		 benign
NM_001242792.2(SNAP91):c.1157-3T>C single nucleotide variant not provided [RCV000975115] Chr6:83601441 [GRCh38]
Chr6:84311160 [GRCh37]
Chr6:6q14.2		 benign
NM_001242792.2(SNAP91):c.2113C>T (p.Pro705Ser) single nucleotide variant not provided [RCV000913348] Chr6:83582258 [GRCh38]
Chr6:84291977 [GRCh37]
Chr6:6q14.2		 benign
NC_000006.11:g.(?_83878953)_(84567108_?)dup duplication not provided [RCV001299718] Chr6:83878953..84567108 [GRCh37]
Chr6:6q14.1-14.2		 uncertain significance
GRCh37/hg19 6q12-16.1(chr6:69938252-94379210) copy number gain not specified [RCV002053581] Chr6:69938252..94379210 [GRCh37]
Chr6:6q12-16.1		 pathogenic
GRCh37/hg19 6q14.1-15(chr6:83141523-88023466)x1 copy number loss not provided [RCV001829074] Chr6:83141523..88023466 [GRCh37]
Chr6:6q14.1-15		 pathogenic
NM_001242792.2(SNAP91):c.1381C>T (p.Pro461Ser) single nucleotide variant not specified [RCV004287610] Chr6:83594425 [GRCh38]
Chr6:84304144 [GRCh37]
Chr6:6q14.2		 uncertain significance
GRCh37/hg19 6q14.1-16.1(chr6:78911022-98909173)x1 copy number loss See cases [RCV002292710] Chr6:78911022..98909173 [GRCh37]
Chr6:6q14.1-16.1		 uncertain significance
GRCh37/hg19 6q14.2-14.3(chr6:84373743-85044270)x3 copy number gain not provided [RCV002473700] Chr6:84373743..85044270 [GRCh37]
Chr6:6q14.2-14.3		 uncertain significance
NM_001242792.2(SNAP91):c.2314G>C (p.Gly772Arg) single nucleotide variant not specified [RCV004170163] Chr6:83576039 [GRCh38]
Chr6:84285758 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.716G>T (p.Arg239Leu) single nucleotide variant not specified [RCV004213130] Chr6:83641145 [GRCh38]
Chr6:84350864 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.502A>G (p.Met168Val) single nucleotide variant not specified [RCV004215368] Chr6:83659043 [GRCh38]
Chr6:84368762 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.836A>C (p.Glu279Ala) single nucleotide variant not specified [RCV004148892] Chr6:83617011 [GRCh38]
Chr6:84326730 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.1843T>C (p.Ser615Pro) single nucleotide variant not specified [RCV004189773] Chr6:83592949 [GRCh38]
Chr6:84302668 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.2615C>G (p.Ala872Gly) single nucleotide variant not specified [RCV004244227] Chr6:83560120 [GRCh38]
Chr6:84269839 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.1870C>T (p.Pro624Ser) single nucleotide variant not specified [RCV004132781] Chr6:83592515 [GRCh38]
Chr6:84302234 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.1429A>G (p.Asn477Asp) single nucleotide variant not specified [RCV004200956] Chr6:83594377 [GRCh38]
Chr6:84304096 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.2402C>T (p.Pro801Leu) single nucleotide variant not specified [RCV004131266] Chr6:83575050 [GRCh38]
Chr6:84284769 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.145A>G (p.Thr49Ala) single nucleotide variant not specified [RCV004155728] Chr6:83665567 [GRCh38]
Chr6:84375286 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.2134T>C (p.Ser712Pro) single nucleotide variant not specified [RCV004234456] Chr6:83582237 [GRCh38]
Chr6:84291956 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.1997C>T (p.Ser666Leu) single nucleotide variant not specified [RCV004230350] Chr6:83591228 [GRCh38]
Chr6:84300947 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.2364G>T (p.Lys788Asn) single nucleotide variant not specified [RCV004148775] Chr6:83575088 [GRCh38]
Chr6:84284807 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.2485G>A (p.Gly829Arg) single nucleotide variant not specified [RCV004188767] Chr6:83560905 [GRCh38]
Chr6:84270624 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.2426C>T (p.Pro809Leu) single nucleotide variant not specified [RCV004143218] Chr6:83575026 [GRCh38]
Chr6:84284745 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.1598C>T (p.Ala533Val) single nucleotide variant not specified [RCV004145238] Chr6:83593576 [GRCh38]
Chr6:84303295 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.1933G>A (p.Ala645Thr) single nucleotide variant not specified [RCV004076919] Chr6:83591292 [GRCh38]
Chr6:84301011 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.2557C>T (p.Pro853Ser) single nucleotide variant not specified [RCV004266692] Chr6:83560178 [GRCh38]
Chr6:84269897 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.1265C>A (p.Ala422Asp) single nucleotide variant not specified [RCV004256809] Chr6:83601330 [GRCh38]
Chr6:84311049 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.419A>G (p.Gln140Arg) single nucleotide variant not specified [RCV004248650] Chr6:83661535 [GRCh38]
Chr6:84371254 [GRCh37]
Chr6:6q14.2		 uncertain significance
GRCh37/hg19 6q14.1-14.3(chr6:82840207-86522229)x1 copy number loss See cases [RCV003222551] Chr6:82840207..86522229 [GRCh37]
Chr6:6q14.1-14.3		 pathogenic
NM_001242792.2(SNAP91):c.1306G>A (p.Glu436Lys) single nucleotide variant not specified [RCV004271639] Chr6:83601289 [GRCh38]
Chr6:84311008 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.2488G>A (p.Ala830Thr) single nucleotide variant not specified [RCV004311522] Chr6:83560902 [GRCh38]
Chr6:84270621 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.355G>A (p.Asp119Asn) single nucleotide variant not specified [RCV004365168] Chr6:83661599 [GRCh38]
Chr6:84371318 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.2651C>A (p.Pro884His) single nucleotide variant not specified [RCV004346743] Chr6:83556226 [GRCh38]
Chr6:84265945 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.1975G>T (p.Ala659Ser) single nucleotide variant not specified [RCV004334844] Chr6:83591250 [GRCh38]
Chr6:84300969 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.1747G>C (p.Ala583Pro) single nucleotide variant not specified [RCV004339816] Chr6:83593209 [GRCh38]
Chr6:84302928 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.1948G>A (p.Ala650Thr) single nucleotide variant not specified [RCV004366155] Chr6:83591277 [GRCh38]
Chr6:84300996 [GRCh37]
Chr6:6q14.2		 uncertain significance
GRCh37/hg19 6q14.2(chr6:83982285-84276653)x3 copy number gain not specified [RCV003986660] Chr6:83982285..84276653 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.766-4799T>C single nucleotide variant not provided [RCV003990107] Chr6:83628141 [GRCh38]
Chr6:84337860 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.1115C>G (p.Pro372Arg) single nucleotide variant not specified [RCV004462250] Chr6:83605711 [GRCh38]
Chr6:84315430 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.1651G>A (p.Ala551Thr) single nucleotide variant not specified [RCV004462254] Chr6:83593523 [GRCh38]
Chr6:84303242 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.2653G>T (p.Ala885Ser) single nucleotide variant not specified [RCV004462262] Chr6:83556224 [GRCh38]
Chr6:84265943 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.1897G>A (p.Val633Met) single nucleotide variant not specified [RCV004462256] Chr6:83592488 [GRCh38]
Chr6:84302207 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.1973A>T (p.Gln658Leu) single nucleotide variant not specified [RCV004462257] Chr6:83591252 [GRCh38]
Chr6:84300971 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.1445C>T (p.Pro482Leu) single nucleotide variant not specified [RCV004462252] Chr6:83593729 [GRCh38]
Chr6:84303448 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.2017T>C (p.Phe673Leu) single nucleotide variant not specified [RCV004462258] Chr6:83582354 [GRCh38]
Chr6:84292073 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.2483C>T (p.Ala828Val) single nucleotide variant not specified [RCV004462261] Chr6:83560907 [GRCh38]
Chr6:84270626 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.510A>G (p.Ile170Met) single nucleotide variant not specified [RCV004462263] Chr6:83659035 [GRCh38]
Chr6:84368754 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.1259C>T (p.Ala420Val) single nucleotide variant not specified [RCV004462251] Chr6:83601336 [GRCh38]
Chr6:84311055 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.1532C>G (p.Thr511Arg) single nucleotide variant not specified [RCV004462253] Chr6:83593642 [GRCh38]
Chr6:84303361 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.2395G>C (p.Val799Leu) single nucleotide variant not specified [RCV004462260] Chr6:83575057 [GRCh38]
Chr6:84284776 [GRCh37]
Chr6:6q14.2		 uncertain significance
NM_001242792.2(SNAP91):c.981G>A (p.Pro327=) single nucleotide variant not specified [RCV004462264] Chr6:83607740 [GRCh38]
Chr6:84317459 [GRCh37]
Chr6:6q14.2		 likely benign
NM_001242792.2(SNAP91):c.166A>G (p.Ile56Val) single nucleotide variant not specified [RCV004363171] Chr6:83665546 [GRCh38]
Chr6:84375265 [GRCh37]
Chr6:6q14.2		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:8480
Count of miRNA genes:1224
Interacting mature miRNAs:1534
Transcripts:ENST00000195649, ENST00000369690, ENST00000369691, ENST00000369694, ENST00000428679, ENST00000437520, ENST00000439399, ENST00000518309, ENST00000518312, ENST00000519133, ENST00000519779, ENST00000519825, ENST00000520213, ENST00000520302, ENST00000521485, ENST00000521616, ENST00000521743, ENST00000521931, ENST00000522248, ENST00000523199, ENST00000523448, ENST00000523484, ENST00000523585, ENST00000523780
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region
D6S1609  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37684,385,517 - 84,385,688UniSTSGRCh37
Build 36684,442,236 - 84,442,407RGDNCBI36
Celera684,818,812 - 84,818,997RGD
Cytogenetic Map6q12UniSTS
Cytogenetic Map6q14.2UniSTS
HuRef681,615,181 - 81,615,352UniSTS
Marshfield Genetic Map692.25RGD
Marshfield Genetic Map692.25UniSTS
Genethon Genetic Map692.4UniSTS
TNG Radiation Hybrid Map640471.0UniSTS
deCODE Assembly Map692.58UniSTS
GeneMap99-GB4 RH Map6369.19UniSTS
Whitehead-YAC Contig Map6 UniSTS
SHGC-110549  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37684,329,055 - 84,329,325UniSTSGRCh37
Build 36684,385,774 - 84,386,044RGDNCBI36
Celera684,762,345 - 84,762,615RGD
Cytogenetic Map6q14.2UniSTS
HuRef681,558,716 - 81,558,986UniSTS
TNG Radiation Hybrid Map640441.0UniSTS
SHGC-112644  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37684,350,816 - 84,351,086UniSTSGRCh37
Build 36684,407,535 - 84,407,805RGDNCBI36
Celera684,784,106 - 84,784,376RGD
Cytogenetic Map6q14.2UniSTS
HuRef681,580,488 - 81,580,758UniSTS
TNG Radiation Hybrid Map640460.0UniSTS
D6S1922  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37684,390,712 - 84,390,913UniSTSGRCh37
Build 36684,447,431 - 84,447,632RGDNCBI36
Celera684,824,022 - 84,824,223RGD
Cytogenetic Map6q14.2UniSTS
HuRef681,620,376 - 81,620,577UniSTS
Whitehead-RH Map6548.1UniSTS
Whitehead-YAC Contig Map6 UniSTS
RH1538  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37684,262,806 - 84,262,924UniSTSGRCh37
Build 36684,319,525 - 84,319,643RGDNCBI36
Celera684,696,095 - 84,696,213RGD
Cytogenetic Map6q14.2UniSTS
HuRef681,492,458 - 81,492,576UniSTS
GeneMap99-GB4 RH Map6373.7UniSTS
D19S703E  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map6q14.2UniSTS
MARC_21740-21741:1023217238:1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37684,269,871 - 84,270,644UniSTSGRCh37
Celera684,703,160 - 84,703,933UniSTS
HuRef681,499,523 - 81,500,296UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component
High
Medium 1 5 276 2 2 2 2482 4 258 38
Low 1456 1225 367 18 221 19 930 764 777 54 703 378 2 1 71 767 1
Below cutoff 814 1441 808 353 929 192 3119 1375 432 154 385 1028 162 1045 1931 2

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001242792 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001242793 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001242794 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001256717 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001256718 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363677 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376675 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376676 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376677 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376678 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376679 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376680 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376681 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376682 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376683 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376684 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376685 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376686 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376687 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376688 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376689 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376690 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376691 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376692 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376693 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376694 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376695 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376696 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376697 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376698 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376699 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376700 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376701 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376702 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376703 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376704 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376705 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376706 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376707 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376708 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376709 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376710 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376711 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376712 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376713 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376714 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376715 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376716 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376717 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376718 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376719 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376720 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376721 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376723 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376726 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376728 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376731 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376733 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376734 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376735 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376736 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376737 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376738 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376739 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376740 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376741 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376742 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_014841 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_164843 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_164844 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_164845 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_164846 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005248770 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006715615 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011536265 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011536266 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011536269 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011536271 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011536273 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011536275 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011536276 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011557 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011558 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011559 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011560 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011562 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011564 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011565 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011566 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011567 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011569 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011570 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011571 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011572 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011573 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011574 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011575 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011576 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011577 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011579 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011580 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011581 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011582 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011583 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011584 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011585 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011586 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011587 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011589 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011590 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024446599 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024446600 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB014556 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF054993 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK289582 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK294556 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK294898 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL109915 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC036650 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC044579 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC060818 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471051 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068272 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR749348 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA110036 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA307867 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA316497 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA323323 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB480068 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF458213 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000195649   ⟹   ENSP00000195649
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl683,552,885 - 83,709,128 (-)Ensembl
RefSeq Acc Id: ENST00000369690   ⟹   ENSP00000358704
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl683,661,507 - 83,708,414 (-)Ensembl
RefSeq Acc Id: ENST00000369691   ⟹   ENSP00000358705
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl683,593,594 - 83,605,803 (-)Ensembl
RefSeq Acc Id: ENST00000369694   ⟹   ENSP00000358708
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl683,552,885 - 83,709,101 (-)Ensembl
RefSeq Acc Id: ENST00000439399   ⟹   ENSP00000400459
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl683,552,885 - 83,709,408 (-)Ensembl
RefSeq Acc Id: ENST00000518309   ⟹   ENSP00000430441
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl683,661,502 - 83,708,189 (-)Ensembl
RefSeq Acc Id: ENST00000518312   ⟹   ENSP00000429937
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl683,552,895 - 83,709,395 (-)Ensembl
RefSeq Acc Id: ENST00000519133
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl683,575,181 - 83,580,506 (-)Ensembl
RefSeq Acc Id: ENST00000519779   ⟹   ENSP00000429429
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl683,659,088 - 83,709,019 (-)Ensembl
RefSeq Acc Id: ENST00000519825   ⟹   ENSP00000431055
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl683,665,514 - 83,708,713 (-)Ensembl
RefSeq Acc Id: ENST00000520213   ⟹   ENSP00000428026
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl683,554,029 - 83,709,393 (-)Ensembl
RefSeq Acc Id: ENST00000520302   ⟹   ENSP00000428511
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl683,552,891 - 83,709,392 (-)Ensembl
RefSeq Acc Id: ENST00000521485   ⟹   ENSP00000429776
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl683,552,880 - 83,709,691 (-)Ensembl
RefSeq Acc Id: ENST00000521616   ⟹   ENSP00000428127
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl683,554,215 - 83,708,809 (-)Ensembl
RefSeq Acc Id: ENST00000521743   ⟹   ENSP00000428215
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl683,552,891 - 83,709,147 (-)Ensembl
RefSeq Acc Id: ENST00000521931   ⟹   ENSP00000430071
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl683,576,047 - 83,707,927 (-)Ensembl
RefSeq Acc Id: ENST00000522248   ⟹   ENSP00000429700
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl683,656,832 - 83,708,879 (-)Ensembl
RefSeq Acc Id: ENST00000523199   ⟹   ENSP00000428592
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl683,686,829 - 83,708,888 (-)Ensembl
RefSeq Acc Id: ENST00000523448   ⟹   ENSP00000430255
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl683,554,051 - 83,592,982 (-)Ensembl
RefSeq Acc Id: ENST00000523484   ⟹   ENSP00000427959
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl683,662,347 - 83,708,718 (-)Ensembl
RefSeq Acc Id: ENST00000523585   ⟹   ENSP00000429950
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl683,686,090 - 83,709,381 (-)Ensembl
RefSeq Acc Id: ENST00000523780
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl683,593,636 - 83,594,528 (-)Ensembl
RefSeq Acc Id: NM_001242792   ⟹   NP_001229721
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
GRCh37684,262,604 - 84,419,127 (-)ENTREZGENE
HuRef681,492,256 - 81,648,799 (-)ENTREZGENE
CHM1_1684,360,208 - 84,516,460 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001242793   ⟹   NP_001229722
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,393 (-)NCBI
GRCh37684,262,604 - 84,419,127 (-)NCBI
HuRef681,492,256 - 81,648,799 (-)ENTREZGENE
CHM1_1684,360,208 - 84,516,740 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,636 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001242794   ⟹   NP_001229723
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,393 (-)NCBI
GRCh37684,262,604 - 84,419,127 (-)NCBI
HuRef681,492,256 - 81,648,799 (-)ENTREZGENE
CHM1_1684,360,208 - 84,516,740 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,636 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001256717   ⟹   NP_001243646
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,393 (-)NCBI
GRCh37684,262,604 - 84,419,127 (-)NCBI
HuRef681,492,256 - 81,648,799 (-)NCBI
CHM1_1684,360,208 - 84,516,740 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,636 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001256718   ⟹   NP_001243647
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
GRCh37684,262,604 - 84,419,127 (-)NCBI
HuRef681,492,256 - 81,648,799 (-)NCBI
CHM1_1684,360,208 - 84,516,133 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001363677   ⟹   NP_001350606
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,708,772 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,015 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376675   ⟹   NP_001363604
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,393 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,636 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376676   ⟹   NP_001363605
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,393 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,636 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376677   ⟹   NP_001363606
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376678   ⟹   NP_001363607
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376679   ⟹   NP_001363608
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376680   ⟹   NP_001363609
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,708,772 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,015 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376681   ⟹   NP_001363610
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,708,772 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,015 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376682   ⟹   NP_001363611
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,708,772 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,015 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376683   ⟹   NP_001363612
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,393 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,636 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376684   ⟹   NP_001363613
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376685   ⟹   NP_001363614
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,393 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,636 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376686   ⟹   NP_001363615
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,393 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,636 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376687   ⟹   NP_001363616
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376688   ⟹   NP_001363617
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376689   ⟹   NP_001363618
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376690   ⟹   NP_001363619
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,708,772 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,015 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376691   ⟹   NP_001363620
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,708,772 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,015 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376692   ⟹   NP_001363621
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,708,772 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,015 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376693   ⟹   NP_001363622
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,393 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,636 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376694   ⟹   NP_001363623
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376695   ⟹   NP_001363624
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,393 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,636 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376696   ⟹   NP_001363625
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376697   ⟹   NP_001363626
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376698   ⟹   NP_001363627
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,708,772 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,015 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376699   ⟹   NP_001363628
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376700   ⟹   NP_001363629
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,708,772 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,015 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376701   ⟹   NP_001363630
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376702   ⟹   NP_001363631
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,393 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,636 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376703   ⟹   NP_001363632
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,393 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,636 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376704   ⟹   NP_001363633
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376705   ⟹   NP_001363634
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376706   ⟹   NP_001363635
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,708,772 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,015 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376707   ⟹   NP_001363636
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,708,772 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,015 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376708   ⟹   NP_001363637
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,393 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,636 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376709   ⟹   NP_001363638
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376710   ⟹   NP_001363639
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376711   ⟹   NP_001363640
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,708,772 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,015 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376712   ⟹   NP_001363641
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376713   ⟹   NP_001363642
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376714   ⟹   NP_001363643
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,708,772 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,015 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376715   ⟹   NP_001363644
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,708,772 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,015 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376716   ⟹   NP_001363645
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376717   ⟹   NP_001363646
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376718   ⟹   NP_001363647
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,393 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,636 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376719   ⟹   NP_001363648
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376720   ⟹   NP_001363649
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,393 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,636 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376721   ⟹   NP_001363650
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376723   ⟹   NP_001363652
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376726   ⟹   NP_001363655
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,708,772 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,015 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376728   ⟹   NP_001363657
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,702,926 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,926,170 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376731   ⟹   NP_001363660
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376733   ⟹   NP_001363662
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376734   ⟹   NP_001363663
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376735   ⟹   NP_001363664
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,708,772 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,015 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376736   ⟹   NP_001363665
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376737   ⟹   NP_001363666
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376738   ⟹   NP_001363667
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376739   ⟹   NP_001363668
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376740   ⟹   NP_001363669
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376741   ⟹   NP_001363670
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,595,110 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,818,343 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376742   ⟹   NP_001363671
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,608,433 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,831,671 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NM_014841   ⟹   NP_055656
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,393 (-)NCBI
GRCh37684,262,604 - 84,419,127 (-)ENTREZGENE
Build 36684,319,332 - 84,475,495 (-)NCBI Archive
HuRef681,492,256 - 81,648,799 (-)ENTREZGENE
CHM1_1684,360,208 - 84,516,740 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,636 (-)NCBI
Sequence:
RefSeq Acc Id: NR_164843
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NR_164844
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NR_164845
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,709,101 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,344 (-)NCBI
Sequence:
RefSeq Acc Id: NR_164846
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,552,885 - 83,708,772 (-)NCBI
T2T-CHM13v2.0684,776,120 - 84,932,015 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001229721 (Get FASTA)   NCBI Sequence Viewer  
  NP_001229722 (Get FASTA)   NCBI Sequence Viewer  
  NP_001229723 (Get FASTA)   NCBI Sequence Viewer  
  NP_001243646 (Get FASTA)   NCBI Sequence Viewer  
  NP_001243647 (Get FASTA)   NCBI Sequence Viewer  
  NP_001350606 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363604 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363605 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363606 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363607 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363608 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363609 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363610 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363611 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363612 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363613 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363614 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363615 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363616 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363617 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363618 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363619 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363620 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363621 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363622 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363623 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363624 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363625 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363626 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363627 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363628 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363629 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363630 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363631 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363632 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363633 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363634 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363635 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363636 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363637 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363638 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363639 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363640 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363641 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363642 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363643 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363644 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363645 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363646 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363647 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363648 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363649 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363650 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363652 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363655 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363657 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363660 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363662 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363663 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363664 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363665 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363666 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363667 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363668 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363669 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363670 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363671 (Get FASTA)   NCBI Sequence Viewer  
  NP_055656 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAC09352 (Get FASTA)   NCBI Sequence Viewer  
  AAH60818 (Get FASTA)   NCBI Sequence Viewer  
  BAA31631 (Get FASTA)   NCBI Sequence Viewer  
  BAF82271 (Get FASTA)   NCBI Sequence Viewer  
  BAH11808 (Get FASTA)   NCBI Sequence Viewer  
  BAH11918 (Get FASTA)   NCBI Sequence Viewer  
  CAH18201 (Get FASTA)   NCBI Sequence Viewer  
  EAW48656 (Get FASTA)   NCBI Sequence Viewer  
  EAW48657 (Get FASTA)   NCBI Sequence Viewer  
  EAW48658 (Get FASTA)   NCBI Sequence Viewer  
  EAW48659 (Get FASTA)   NCBI Sequence Viewer  
  EAW48660 (Get FASTA)   NCBI Sequence Viewer  
  EAW48661 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000195649
  ENSP00000195649.6
  ENSP00000358704.2
  ENSP00000358705.5
  ENSP00000358708
  ENSP00000358708.2
  ENSP00000400459
  ENSP00000400459.2
  ENSP00000427959.2
  ENSP00000428026
  ENSP00000428026.1
  ENSP00000428127.1
  ENSP00000428215.1
  ENSP00000428511
  ENSP00000428511.1
  ENSP00000428592.1
  ENSP00000429429.1
  ENSP00000429700.1
  ENSP00000429776.1
  ENSP00000429937.1
  ENSP00000429950.1
  ENSP00000430071.1
  ENSP00000430255.1
  ENSP00000430441.1
  ENSP00000431055.1
GenBank Protein O60641 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_001229723   ⟸   NM_001242794
- Peptide Label: isoform c
- UniProtKB: O60641 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001229722   ⟸   NM_001242793
- Peptide Label: isoform b
- UniProtKB: O60641 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_055656   ⟸   NM_014841
- Peptide Label: isoform a
- UniProtKB: Q6P9D3 (UniProtKB/Swiss-Prot),   Q68DL9 (UniProtKB/Swiss-Prot),   Q5JX13 (UniProtKB/Swiss-Prot),   E5RI02 (UniProtKB/Swiss-Prot),   A8K0L7 (UniProtKB/Swiss-Prot),   Q9NTY7 (UniProtKB/Swiss-Prot),   O60641 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001229721   ⟸   NM_001242792
- Peptide Label: isoform a
- UniProtKB: Q6P9D3 (UniProtKB/Swiss-Prot),   Q68DL9 (UniProtKB/Swiss-Prot),   Q5JX13 (UniProtKB/Swiss-Prot),   E5RI02 (UniProtKB/Swiss-Prot),   A8K0L7 (UniProtKB/Swiss-Prot),   Q9NTY7 (UniProtKB/Swiss-Prot),   O60641 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001243646   ⟸   NM_001256717
- Peptide Label: isoform d
- UniProtKB: O60641 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001243647   ⟸   NM_001256718
- Peptide Label: isoform e
- UniProtKB: B7Z2N2 (UniProtKB/TrEMBL),   B7Z2C2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001350606   ⟸   NM_001363677
- Peptide Label: isoform f
- UniProtKB: E9PDG8 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001363624   ⟸   NM_001376695
- Peptide Label: isoform l
RefSeq Acc Id: NP_001363631   ⟸   NM_001376702
- Peptide Label: isoform o
RefSeq Acc Id: NP_001363614   ⟸   NM_001376685
- Peptide Label: isoform i
RefSeq Acc Id: NP_001363605   ⟸   NM_001376676
- Peptide Label: isoform g
RefSeq Acc Id: NP_001363649   ⟸   NM_001376720
- Peptide Label: isoform v
RefSeq Acc Id: NP_001363622   ⟸   NM_001376693
- Peptide Label: isoform j
RefSeq Acc Id: NP_001363612   ⟸   NM_001376683
- Peptide Label: isoform h
RefSeq Acc Id: NP_001363647   ⟸   NM_001376718
- Peptide Label: isoform t
RefSeq Acc Id: NP_001363632   ⟸   NM_001376703
- Peptide Label: isoform o
RefSeq Acc Id: NP_001363637   ⟸   NM_001376708
- Peptide Label: isoform b
RefSeq Acc Id: NP_001363615   ⟸   NM_001376686
- Peptide Label: isoform i
RefSeq Acc Id: NP_001363604   ⟸   NM_001376675
- Peptide Label: isoform g
RefSeq Acc Id: NP_001363668   ⟸   NM_001376739
- Peptide Label: isoform cc
RefSeq Acc Id: NP_001363665   ⟸   NM_001376736
- Peptide Label: isoform z
RefSeq Acc Id: NP_001363645   ⟸   NM_001376716
- Peptide Label: isoform r
RefSeq Acc Id: NP_001363626   ⟸   NM_001376697
- Peptide Label: isoform l
RefSeq Acc Id: NP_001363669   ⟸   NM_001376740
- Peptide Label: isoform dd
- UniProtKB: E5RGY9 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001363662   ⟸   NM_001376733
- Peptide Label: isoform x
RefSeq Acc Id: NP_001363641   ⟸   NM_001376712
- Peptide Label: isoform hh
RefSeq Acc Id: NP_001363660   ⟸   NM_001376731
- Peptide Label: isoform w
RefSeq Acc Id: NP_001363633   ⟸   NM_001376704
- Peptide Label: isoform o
RefSeq Acc Id: NP_001363638   ⟸   NM_001376709
- Peptide Label: isoform b
RefSeq Acc Id: NP_001363617   ⟸   NM_001376688
- Peptide Label: isoform i
RefSeq Acc Id: NP_001363606   ⟸   NM_001376677
- Peptide Label: isoform g
RefSeq Acc Id: NP_001363652   ⟸   NM_001376723
- Peptide Label: isoform v
RefSeq Acc Id: NP_001363646   ⟸   NM_001376717
- Peptide Label: isoform s
RefSeq Acc Id: NP_001363630   ⟸   NM_001376701
- Peptide Label: isoform n
RefSeq Acc Id: NP_001363625   ⟸   NM_001376696
- Peptide Label: isoform l
RefSeq Acc Id: NP_001363667   ⟸   NM_001376738
- Peptide Label: isoform bb
RefSeq Acc Id: NP_001363666   ⟸   NM_001376737
- Peptide Label: isoform aa
RefSeq Acc Id: NP_001363663   ⟸   NM_001376734
- Peptide Label: isoform x
RefSeq Acc Id: NP_001363616   ⟸   NM_001376687
- Peptide Label: isoform gg
RefSeq Acc Id: NP_001363613   ⟸   NM_001376684
- Peptide Label: isoform h
RefSeq Acc Id: NP_001363648   ⟸   NM_001376719
- Peptide Label: isoform u
RefSeq Acc Id: NP_001363642   ⟸   NM_001376713
- Peptide Label: isoform p
RefSeq Acc Id: NP_001363634   ⟸   NM_001376705
- Peptide Label: isoform o
RefSeq Acc Id: NP_001363623   ⟸   NM_001376694
- Peptide Label: isoform k
RefSeq Acc Id: NP_001363639   ⟸   NM_001376710
- Peptide Label: isoform b
RefSeq Acc Id: NP_001363628   ⟸   NM_001376699
- Peptide Label: isoform m
RefSeq Acc Id: NP_001363618   ⟸   NM_001376689
- Peptide Label: isoform i
RefSeq Acc Id: NP_001363607   ⟸   NM_001376678
- Peptide Label: isoform g
RefSeq Acc Id: NP_001363650   ⟸   NM_001376721
- Peptide Label: isoform v
RefSeq Acc Id: NP_001363608   ⟸   NM_001376679
- Peptide Label: isoform g
RefSeq Acc Id: NP_001363655   ⟸   NM_001376726
- Peptide Label: isoform v
RefSeq Acc Id: NP_001363627   ⟸   NM_001376698
- Peptide Label: isoform l
RefSeq Acc Id: NP_001363643   ⟸   NM_001376714
- Peptide Label: isoform p
RefSeq Acc Id: NP_001363635   ⟸   NM_001376706
- Peptide Label: isoform o
RefSeq Acc Id: NP_001363629   ⟸   NM_001376700
- Peptide Label: isoform m
RefSeq Acc Id: NP_001363619   ⟸   NM_001376690
- Peptide Label: isoform i
RefSeq Acc Id: NP_001363609   ⟸   NM_001376680
- Peptide Label: isoform g
RefSeq Acc Id: NP_001363664   ⟸   NM_001376735
- Peptide Label: isoform y
RefSeq Acc Id: NP_001363620   ⟸   NM_001376691
- Peptide Label: isoform i
RefSeq Acc Id: NP_001363636   ⟸   NM_001376707
- Peptide Label: isoform o
RefSeq Acc Id: NP_001363640   ⟸   NM_001376711
- Peptide Label: isoform b
RefSeq Acc Id: NP_001363621   ⟸   NM_001376692
- Peptide Label: isoform i
RefSeq Acc Id: NP_001363610   ⟸   NM_001376681
- Peptide Label: isoform g
RefSeq Acc Id: NP_001363644   ⟸   NM_001376715
- Peptide Label: isoform q
RefSeq Acc Id: NP_001363611   ⟸   NM_001376682
- Peptide Label: isoform g
RefSeq Acc Id: NP_001363657   ⟸   NM_001376728
- Peptide Label: isoform v
RefSeq Acc Id: NP_001363670   ⟸   NM_001376741
- Peptide Label: isoform ee
RefSeq Acc Id: NP_001363671   ⟸   NM_001376742
- Peptide Label: isoform ff
RefSeq Acc Id: ENSP00000400459   ⟸   ENST00000439399
RefSeq Acc Id: ENSP00000429937   ⟸   ENST00000518312
RefSeq Acc Id: ENSP00000430441   ⟸   ENST00000518309
RefSeq Acc Id: ENSP00000429429   ⟸   ENST00000519779
RefSeq Acc Id: ENSP00000431055   ⟸   ENST00000519825
RefSeq Acc Id: ENSP00000428511   ⟸   ENST00000520302
RefSeq Acc Id: ENSP00000428026   ⟸   ENST00000520213
RefSeq Acc Id: ENSP00000428215   ⟸   ENST00000521743
RefSeq Acc Id: ENSP00000428127   ⟸   ENST00000521616
RefSeq Acc Id: ENSP00000429776   ⟸   ENST00000521485
RefSeq Acc Id: ENSP00000430071   ⟸   ENST00000521931
RefSeq Acc Id: ENSP00000429700   ⟸   ENST00000522248
RefSeq Acc Id: ENSP00000429950   ⟸   ENST00000523585
RefSeq Acc Id: ENSP00000430255   ⟸   ENST00000523448
RefSeq Acc Id: ENSP00000427959   ⟸   ENST00000523484
RefSeq Acc Id: ENSP00000428592   ⟸   ENST00000523199
RefSeq Acc Id: ENSP00000195649   ⟸   ENST00000195649
RefSeq Acc Id: ENSP00000358708   ⟸   ENST00000369694
RefSeq Acc Id: ENSP00000358705   ⟸   ENST00000369691
RefSeq Acc Id: ENSP00000358704   ⟸   ENST00000369690
Protein Domains
AP180 N-terminal homology (ANTH)   ENTH

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-O60641-F1-model_v2 AlphaFold O60641 1-907 view protein structure

Promoters
RGD ID:7208593
Promoter ID:EPDNEW_H10042
Type:initiation region
Name:SNAP91_2
Description:synaptosome associated protein 91
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H10043  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,709,082 - 83,709,142EPDNEW
RGD ID:7208595
Promoter ID:EPDNEW_H10043
Type:initiation region
Name:SNAP91_1
Description:synaptosome associated protein 91
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H10042  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38683,709,393 - 83,709,453EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:14986 AgrOrtholog
COSMIC SNAP91 COSMIC
Ensembl Genes ENSG00000065609 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000195649 ENTREZGENE
  ENST00000195649.10 UniProtKB/TrEMBL
  ENST00000369690.6 UniProtKB/TrEMBL
  ENST00000369691.5 UniProtKB/TrEMBL
  ENST00000369694 ENTREZGENE
  ENST00000369694.7 UniProtKB/Swiss-Prot
  ENST00000439399 ENTREZGENE
  ENST00000439399.6 UniProtKB/Swiss-Prot
  ENST00000518309.6 UniProtKB/TrEMBL
  ENST00000518312 ENTREZGENE
  ENST00000518312.5 UniProtKB/TrEMBL
  ENST00000519779.5 UniProtKB/TrEMBL
  ENST00000519825.5 UniProtKB/TrEMBL
  ENST00000520213 ENTREZGENE
  ENST00000520213.5 UniProtKB/Swiss-Prot
  ENST00000520302 ENTREZGENE
  ENST00000520302.5 UniProtKB/Swiss-Prot
  ENST00000521485.5 UniProtKB/TrEMBL
  ENST00000521616.5 UniProtKB/TrEMBL
  ENST00000521743.5 UniProtKB/Swiss-Prot
  ENST00000521931.5 UniProtKB/TrEMBL
  ENST00000522248.5 UniProtKB/TrEMBL
  ENST00000523199.1 UniProtKB/TrEMBL
  ENST00000523448.5 UniProtKB/TrEMBL
  ENST00000523484.6 UniProtKB/TrEMBL
  ENST00000523585.5 UniProtKB/TrEMBL
Gene3D-CATH 1.20.58.150 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  1.25.40.90 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000065609 GTEx
HGNC ID HGNC:14986 ENTREZGENE
Human Proteome Map SNAP91 Human Proteome Map
InterPro ANTH_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  AP180-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Clathrin_AP_dom2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENTH UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENTH_VHS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:9892 UniProtKB/Swiss-Prot
NCBI Gene 9892 ENTREZGENE
OMIM 607923 OMIM
PANTHER PTHR22951 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR22951:SF4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam ANTH UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA37956 PharmGKB
PROSITE ENTH UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART ENTH UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP GAT-like domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF48464 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A0A0MRM7_HUMAN UniProtKB/TrEMBL
  A8K0L7 ENTREZGENE
  AP180_HUMAN UniProtKB/Swiss-Prot
  B7Z2C2 ENTREZGENE, UniProtKB/TrEMBL
  B7Z2N2 ENTREZGENE, UniProtKB/TrEMBL
  E5RFC6_HUMAN UniProtKB/TrEMBL
  E5RFU0_HUMAN UniProtKB/TrEMBL
  E5RGP8_HUMAN UniProtKB/TrEMBL
  E5RGY9 ENTREZGENE, UniProtKB/TrEMBL
  E5RHK9_HUMAN UniProtKB/TrEMBL
  E5RI02 ENTREZGENE
  E5RIJ5_HUMAN UniProtKB/TrEMBL
  E5RJY3_HUMAN UniProtKB/TrEMBL
  E5RK51_HUMAN UniProtKB/TrEMBL
  E5RK53_HUMAN UniProtKB/TrEMBL
  E9PDG8 ENTREZGENE, UniProtKB/TrEMBL
  H0YBT2_HUMAN UniProtKB/TrEMBL
  O60641 ENTREZGENE
  Q5JX13 ENTREZGENE
  Q68DL9 ENTREZGENE
  Q6P9D3 ENTREZGENE
  Q9NTY7 ENTREZGENE
UniProt Secondary A8K0L7 UniProtKB/Swiss-Prot
  E5RI02 UniProtKB/Swiss-Prot
  Q5JX13 UniProtKB/Swiss-Prot
  Q68DL9 UniProtKB/Swiss-Prot
  Q6P9D3 UniProtKB/Swiss-Prot
  Q9NTY7 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-06-07 SNAP91  synaptosome associated protein 91    synaptosome associated protein 91kDa  Symbol and/or name change 5135510 APPROVED
2015-11-17 SNAP91  synaptosome associated protein 91kDa    synaptosomal-associated protein, 91kDa  Symbol and/or name change 5135510 APPROVED
2012-12-12 SNAP91  synaptosomal-associated protein, 91kDa    synaptosomal-associated protein, 91kDa homolog (mouse)  Symbol and/or name change 5135510 APPROVED